- Trials with a EudraCT protocol (1,490)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (35)
1,490 result(s) found for: White.
Displaying page 1 of 75.
EudraCT Number: 2005-005184-29 | Sponsor Protocol Number: P305-R-EG04 | Start Date*: 2006-02-21 |
Sponsor Name:GABA GmbH | ||
Full Title: Prevention of incipient carious lesions (white spot lesions) in patients with fixed orthodontic appliances following the application of elmex® gelée | ||
Medical condition: incipient carious lesions (white spot lesions) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-004792-14 | Sponsor Protocol Number: 0298-21 | Start Date*: 2021-09-08 | |||||||||||
Sponsor Name:Intas Pharmaceuticals Ltd. | |||||||||||||
Full Title: A Randomized, Active-Controlled, Multicenter, Open label, Two Arm Study to Assess Safety, Efficacy, Pharmacodynamics, and Pharmacokinetics with Pegfilgrastim PFS of Intas Pharmaceutical Limited Com... | |||||||||||||
Medical condition: Paediatric Patients Under 6 years of Age with Rhabdomyosarcoma or Wilms’ Tumour on Myelosuppressive Chemotherapy (CmT) Regimen | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000363-20 | Sponsor Protocol Number: 25433925 | Start Date*: 2007-05-03 | |||||||||||
Sponsor Name:Ritva Nissi | |||||||||||||
Full Title: Kalsineuriini-inhibiittori pimekrolimuusin aikaansaamat histologiset muutokset valkojäkälän paranemisvaiheessa | |||||||||||||
Medical condition: valkojäkälä (lichen slerosus) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015640-42 | Sponsor Protocol Number: PDT02 | Start Date*: 2009-09-29 | ||||||||||||||||
Sponsor Name: | ||||||||||||||||||
Full Title: Etude de l’efficacité thérapeutique de la photothérapie dynamique (PDT) dans le lichen scléreux génital et les dysplasies génitales résistantes aux traitements conventionnels. | ||||||||||||||||||
Medical condition: lichen sclerosus genital dysplasia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014833-26 | Sponsor Protocol Number: IEO S500/409 | Start Date*: 2010-07-29 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Phase IIB Randomized, Placebo Controlled Trial of Pioglitazone for Oral Premalignant Lesions. An Inter-Consortium Collaborative Study. | |||||||||||||
Medical condition: oral premalignant lesions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020538-24 | Sponsor Protocol Number: GASAS-1002X | Start Date*: 2011-02-16 |
Sponsor Name:GABA International AG | ||
Full Title: White spot lesion development in post-orthodontic patients following weekly application of a 1.25% fluoride gel compared to placebo over 6 months | ||
Medical condition: To monitor the white spot lesion development and dental status under weekly applied 1.25% fluoride gel compared to placebo in patients after orthodontic treatment with multibracket appliances | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-012275-98 | Sponsor Protocol Number: HELENA | Start Date*: 2010-09-08 |
Sponsor Name:Free state of Bavaria | ||
Full Title: HEXVIX® VERUS WHITE LIGHT GUIDED TURB FOR EORTC SCORE INTERMEDIATE RISK NON-MUSCLE INVASIVE BLADDER CANCER FOLLOWED BY ATTENUATED INTRAVESICAL ADJUVANT CHEMOTHERAPY. | ||
Medical condition: NON-MUSCLE INVASIVE BLADDER CANCER | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) AT (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2004-002259-15 | Sponsor Protocol Number: PCB305/04 | Start Date*: 2005-01-24 | |||||||||||
Sponsor Name:Photocure ASA | |||||||||||||
Full Title: A RANDOMIZED, COMPARATIVE,CONTROLLED PHASE III, MULTICENTER STUDY OF HEXVIX FLUORESCENCE CYSTOSCOPY ANDWHITE LIGHT CYSTOSCOPY IN THE DETECTION OF PAPILLARY BLADDER CANCER AND THE EARLYRECURRENCE RA... | |||||||||||||
Medical condition: Malignant neoplasm of bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004004-22 | Sponsor Protocol Number: 233928 | Start Date*: 2018-03-16 |
Sponsor Name:University of Sussex | ||
Full Title: A Multi-Centred, Open Label, Randomised Study Assessing the Cardiovascular Outcomes Following Treatment of White Coat Hypertension with Established Anti-Hypertensive Drugs versus Standard of Care i... | ||
Medical condition: White Coat Hypertension | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-001438-25 | Sponsor Protocol Number: VWM1 | Start Date*: 2020-04-21 |
Sponsor Name:VU University Medical Center | ||
Full Title: A Study to Explore the Safety, Tolerability, Pharmacokinetic Profile, and Potential Efficacy of Guanabenz in Patients With Early Childhood Onset Vanishing White Matter (VWM) | ||
Medical condition: Vanishing white matter | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000237-48 | Sponsor Protocol Number: MiraBAT01 | Start Date*: 2016-04-20 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: The effect of Mirabegron on brown adipose tissue in healthy young white Caucasian and South Asian men | ||
Medical condition: Obesity and dyslipidemia | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002982-30 | Sponsor Protocol Number: AGO/2008/004 | Start Date*: 2008-10-09 |
Sponsor Name:University Hospital Ghent | ||
Full Title: A Prospective, randomized, clinical study on the effects of CPP-ACP paste on plaque, gingivitis and initial caries lesion development in orthodontic patients - part 2 | ||
Medical condition: Plaque and the initial development of caries and gingivitis in orthodontic patients. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004269-34 | Sponsor Protocol Number: PCB202/11 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Photocure ASA | |||||||||||||
Full Title: An open, prospective, within-patient, controlled, multi-center phase IIa study of Hexvix flexible fluorescence cystoscopy and white light flexible cystoscopy in the detection of bladder cancer afte... | |||||||||||||
Medical condition: The patients should be indicated for a transurethral resection of the bladder (TURB) based on an outpatient cystoscopy and fulfil the following inclusion criteria: • Patients with multiple bladder... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003622-16 | Sponsor Protocol Number: T214/2016 | Start Date*: 2017-09-19 |
Sponsor Name:Turku University Hospital | ||
Full Title: Targeting SPMS: Effect of teriflunomide treatment on microglial activation in an MS patient cohort at risk of progression. A [11C]PK11195 Brain PET study. | ||
Medical condition: Multiple sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000373-80 | Sponsor Protocol Number: DERM-101 | Start Date*: 2018-05-24 | ||||||||||||||||
Sponsor Name:Dermecular Therapeutics, Inc. | ||||||||||||||||||
Full Title: A Phase 1/2, Randomized, Double-Blind, Placebo-Controlled, Parallel-Arm Study of the Safety and Efficacy of LX3305, a Sphingosine-1-Phosphate Lyase Inhibitor, for Treatment of Darier’s Disease or H... | ||||||||||||||||||
Medical condition: Darier’s Disease or Hailey-Hailey Disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000238-23 | Sponsor Protocol Number: ExeBAT01 | Start Date*: 2016-08-09 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: The effect of Exenatide on brown adipose tissue activity and energy expenditure in healthy young men | ||
Medical condition: Healthy volunteers, intended indications: obesity and dyslipidemia | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002512-27 | Sponsor Protocol Number: NL44774.068.13 | Start Date*: 2013-11-25 |
Sponsor Name:Maastricht University | ||
Full Title: The role of bile acids in human brown adipose tissue metabolism | ||
Medical condition: Healthy subjects | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005815-10 | Sponsor Protocol Number: AJSEB001 | Start Date*: 2012-05-31 | |||||||||||||||||||||
Sponsor Name:Newcastle Upon Tyne Hospitals NHS Foundation Trust | |||||||||||||||||||||||
Full Title: Developmental Clinical Sciences: Does GM-CSF restore effective neutrophil function in critically ill patients? | |||||||||||||||||||||||
Medical condition: Complement mediated dysfunctional neutrophil phagocytosis in critical illness. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002026-39 | Sponsor Protocol Number: N15LDC | Start Date*: 2015-09-10 |
Sponsor Name:NKI-AVL | ||
Full Title: The Effect of Prehydration on the Pharmacokinetics of Low-dose Cisplatin | ||
Medical condition: Tumor | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001542-17 | Sponsor Protocol Number: T109/2019Xe-SAH | Start Date*: 2020-09-17 | |||||||||||
Sponsor Name:Timo Laitio | |||||||||||||
Full Title: Effect of xenon on brain injury, neurological outcome and survival in patients after aneurysmal subarachnoid hemorrhage | |||||||||||||
Medical condition: Acute rupture of cerebral aneurysm, subarachnoid hemorrhage (SAH), unconsciousness, brain injury. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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